2578-41-8 Usage
Physical appearance
White crystalline powder This describes the solid form of 1H-Imidazole-1-carboxamide, which appears as a white, crystalline substance.
Pharmaceutical industry use
Building block for drug synthesis 1H-Imidazole-1-carboxamide is commonly used as a starting material in the synthesis of various drugs, including antifungal and antiparasitic agents.
Corrosion inhibition
Potential use in industrial applications Due to its ability to form stable complexes with metal ions, 1H-Imidazole-1-carboxamide has been studied for its potential as a corrosion inhibitor in various industries.
Flame retardant potential
Investigated for its fire-resistant properties 1H-Imidazole-1-carboxamide has been researched for its possible use as a flame retardant, which could make it a valuable component in fire safety applications.
Precursor for functional materials
Synthesis of advanced materials As a versatile chemical, 1H-Imidazole-1-carboxamide can be used as a precursor for the synthesis of various functional materials with potential applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 2578-41-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,7 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2578-41:
(6*2)+(5*5)+(4*7)+(3*8)+(2*4)+(1*1)=98
98 % 10 = 8
So 2578-41-8 is a valid CAS Registry Number.
2578-41-8Relevant articles and documents
3-(1-Hydroxyalkyl)-1,4,2-dioxazol-5-ones and 3-Hydroxyoxazolidine-2,4-diones from 2-Hydroxycarbohydroxamic Acids and 1,1'-Carbonyldiimidazole
Geffken, Detlef
, p. 211 - 218 (2007/10/02)
The reaction of 2-hydroxycarbohydroxamic acids 6 with 1,1'-carbonyldiimidazole produces 3-(1-hydroxyalkyl)-1,4,2-dioxazol-5-ones 7 and 3-hydroxyoxazolidine-2,4-diones 8.The formation of the heterocycles 7 and 8 depends largely on the substitution at C-2 of 6.Excess of imidazole causes rapid decomposition of 7 into carbonyl compound 9 and isocyanic acid, which yields the adduct 10 with imidazole.Benzylaminolysis of 7a gives 11 whereas the reaction of 7a with 3-chloroaniline produces the ureas 12 and 14 and benzophenone (9a).From the reaction of 7a with imidazole in a mole ratio of 1 : 1 the decomposition products 9a and 10 and 3-hydroxy-5,5-diphenyloxazolidine-2,4-dione (8a) are obtained.